Tariq Ahmad Sheikh , Shahid Yousuf Ganie , Darakhshan Javaid , Deepa Yadav , Mohd Salim Reshi
{"title":"芹菜:植物化学分析和细胞毒性评估","authors":"Tariq Ahmad Sheikh , Shahid Yousuf Ganie , Darakhshan Javaid , Deepa Yadav , Mohd Salim Reshi","doi":"10.1016/j.prenap.2024.100075","DOIUrl":null,"url":null,"abstract":"<div><p><em>Apium leptophyllum</em> (<em>AL</em>) has significantly been used in traditional medicine. The present study was planned to evaluate the phytochemical screening and anti-proleferative potential of <em>AL</em> seed extract. Phytochemical analysis of seed extract was performed by HPLC and FTIR. Furthermore, anti-proliferative potential of ethanolic extract of <em>AL</em> seeds was evaluated on five different cell lines by using the MTT assay. Colony formation assay of ethanolic extract of <em>AL</em> seeds was checked on MCF-7 and A549 cancer cells. DAPI was performed to evaluate the induction of apoptosis by <em>AL</em> extract on MCF-7 cells. The HPLC analysis of ethanolic extract of <em>AL</em> showed presence of Thymol as main constituent. The FTIR analysis of ethanolic extract of <em>AL</em> showed presence of alcohols, carboxylic acids, alkanes, ketones etc. The results of anti-proliferative assay of ethanolic extract of <em>AL</em> showed concentration dependent antiproliferative activity on each cell line. The antiproliferative efficacy of <em>AL</em> was seen more in breast cancer cells (MCF-7) and lung cancer cells (A549) and least effect was shown on liver cancer cell line. Colony formation assay showed concentration dependent inhibition. By performing apoptotic assay on MCF-7 cell line using DAPI dye. <em>AL</em> treated cells showed apoptotic changes such as cell shrinkage, membrane blebbing, chromatin condensation and nuclear fragmentation. The current study confirms the potential bioactivity of the plant being investigated. Consequently, with continued pre-clinical and clinical research, this study could contribute to the development of a safe, affordable, and effective anticancer medication for the well-being of individuals.</p></div>","PeriodicalId":101014,"journal":{"name":"Pharmacological Research - Natural Products","volume":"4 ","pages":"Article 100075"},"PeriodicalIF":0.0000,"publicationDate":"2024-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Apium leptophyllum: Phytochemical analysis and cytotoxicity evaluation\",\"authors\":\"Tariq Ahmad Sheikh , Shahid Yousuf Ganie , Darakhshan Javaid , Deepa Yadav , Mohd Salim Reshi\",\"doi\":\"10.1016/j.prenap.2024.100075\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><em>Apium leptophyllum</em> (<em>AL</em>) has significantly been used in traditional medicine. 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The antiproliferative efficacy of <em>AL</em> was seen more in breast cancer cells (MCF-7) and lung cancer cells (A549) and least effect was shown on liver cancer cell line. Colony formation assay showed concentration dependent inhibition. By performing apoptotic assay on MCF-7 cell line using DAPI dye. <em>AL</em> treated cells showed apoptotic changes such as cell shrinkage, membrane blebbing, chromatin condensation and nuclear fragmentation. The current study confirms the potential bioactivity of the plant being investigated. 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引用次数: 0
摘要
芹属植物(AL)在传统医学中的应用非常广泛。本研究计划评估芹菜种子提取物的植物化学筛选和抗干扰潜力。通过高效液相色谱法和傅立叶变换红外光谱法对种子提取物进行了植物化学分析。此外,还使用 MTT 法评估了 AL 种子乙醇提取物对五种不同细胞系的抗增殖潜力。在 MCF-7 和 A549 癌细胞上检测了 AL 种子乙醇提取物的集落形成试验。DAPI 用于评估 AL 提取物对 MCF-7 细胞凋亡的诱导作用。AL 乙醇提取物的 HPLC 分析表明其主要成分为百里酚。AL 乙醇提取物的傅立叶变换红外光谱分析显示了醇、羧酸、烷、酮等成分的存在。AL 乙醇提取物的抗增殖试验结果表明,它对每种细胞系的抗增殖活性都具有浓度依赖性。AL 对乳腺癌细胞(MCF-7)和肺癌细胞(A549)的抗增殖效果较强,而对肝癌细胞株的作用最小。集落形成试验显示了浓度依赖性抑制作用。使用 DAPI 染料对 MCF-7 细胞系进行凋亡检测。经 AL 处理的细胞出现了凋亡变化,如细胞萎缩、膜脱落、染色质凝结和核破碎。目前的研究证实了所研究植物的潜在生物活性。因此,随着临床前和临床研究的不断深入,这项研究将有助于开发安全、经济、有效的抗癌药物,造福人类。
Apium leptophyllum: Phytochemical analysis and cytotoxicity evaluation
Apium leptophyllum (AL) has significantly been used in traditional medicine. The present study was planned to evaluate the phytochemical screening and anti-proleferative potential of AL seed extract. Phytochemical analysis of seed extract was performed by HPLC and FTIR. Furthermore, anti-proliferative potential of ethanolic extract of AL seeds was evaluated on five different cell lines by using the MTT assay. Colony formation assay of ethanolic extract of AL seeds was checked on MCF-7 and A549 cancer cells. DAPI was performed to evaluate the induction of apoptosis by AL extract on MCF-7 cells. The HPLC analysis of ethanolic extract of AL showed presence of Thymol as main constituent. The FTIR analysis of ethanolic extract of AL showed presence of alcohols, carboxylic acids, alkanes, ketones etc. The results of anti-proliferative assay of ethanolic extract of AL showed concentration dependent antiproliferative activity on each cell line. The antiproliferative efficacy of AL was seen more in breast cancer cells (MCF-7) and lung cancer cells (A549) and least effect was shown on liver cancer cell line. Colony formation assay showed concentration dependent inhibition. By performing apoptotic assay on MCF-7 cell line using DAPI dye. AL treated cells showed apoptotic changes such as cell shrinkage, membrane blebbing, chromatin condensation and nuclear fragmentation. The current study confirms the potential bioactivity of the plant being investigated. Consequently, with continued pre-clinical and clinical research, this study could contribute to the development of a safe, affordable, and effective anticancer medication for the well-being of individuals.